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Association of SCNN1A Single Nucleotide Polymorphisms with neonatal respiratory distress syndrome
Increasing evidence has demonstrated that lung fluid absorption disorders might be an important cause of neonatal respiratory distress syndrome (RDS) by influencing gas exchange or surfactant function. The SCNN1A gene, which encodes the α-ENaC, might predispose infants to RDS. To explore whether the...
Enregistré dans:
| Publié dans: | Sci Rep |
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| Auteurs principaux: | , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Nature Publishing Group
2015
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4661423/ https://ncbi.nlm.nih.gov/pubmed/26611714 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep17317 |
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